Cvs Daytime Cold And Flu Relief And Nighttime Cold And Flu Relief
Product Images NDC 69842-070

2 FDA label images from Cvs Pharmacy, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Cvs Daytime Cold And Flu Relief And Nighttime Cold And Flu Relief (NDC 69842-070). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cvs Pharmacy, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Cvs Day Night Cold Flu Back

Cvs Day   Night Cold   Flu Back
Drug Facts text panels for CVS Daytime COLD and FLU RELIEF and Nighttime COLD and FLU RELIEF. The image shows two separate sections with active ingredients, uses, warnings, directions, and other typical drug facts information for each product variant. The panels provide consumer guidance and safety information for cold and flu symptom relief products by CVS Pharmacy, Inc.*
FDA Label Image

Cvs Day Night Cold Flu Front

Cvs Day   Night Cold   Flu Front
The packaging label for CVS Daytime COLD and FLU RELIEF and Nighttime COLD and FLU RELIEF shows two products: Daytime Severe Cold & Flu Relief in orange and Nighttime Severe Cold & Flu Relief in dark blue. The label includes detailed drug facts panels with active ingredients, uses, warnings, directions, and other information. The Daytime formula contains acetaminophen, dextromethorphan HBr, and phenylephrine HCl, while the Nighttime formula contains acetaminophen, diphenhydramine HCl, and phenylephrine HCl. Each product contains 12 softgels and is labeled as CVS Health with product codes and a UPC barcode.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.